HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Chlorobenzaldehyde → HCID 178504058, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Chlorobenzaldehyde | HCID 7726 | — |
| Reactant | 3,4-Dichlorobenzaldehyde | HCID 22710 | — |
| Reactant | 4-Cyanobenzaldehyde | HCID 66042 | — |
| Reactant | HCID 178419558 | HCID 178419558 | — |
| Reactant | HCID 178419559 | HCID 178419559 | — |
| Reactant | HCID 178477488 | HCID 178477488 | — |
| Reactant | HCID 178477489 | HCID 178477489 | — |
| Reactant | Methyl hydrazinecarbimidothioate | HCID 178504051 | — |
| Reactant | HCID 178504057 | HCID 178504057 | — |
| Product | HCID 178504058 | HCID 178504058 | — |
Reaction Steps
The following are prepared in like manner: methyl 3-(4-bromobenzylidene)thiocarbazimidate methosulfate from 4-chlorobenzaldehyde and methyl thiocarbazimidate methosulfate, ethyl 3-(4-cyanobenzylidene)thiocarbazimidate hydroiodide from 4-cyanobenzaldehyde and ethyl thiocarbazimidate hydroiodide, and propyl 3-(3,4-dichlorobenzylidene)thiocarbazimidate hydrobromide from 3,4-dichlorobenzaldehyde and propyl thiocarbazimidate hydrobromide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03992446 |
| Source dataset | uspto-grants-1976_11 |
| ORD ID | ord-de8e5c08fd3b42efa4e4a01f2d06e745 |
| Source note | uspto-grants-1976_11 |